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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137016copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,087,605-220,101,994 , GRCh38.p12 chr1: 219,914,263-219,928,652 SLC30A10, LOC107985281
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095973copy number variation1nstd102humanPathogenic GRCh37 chr1: 220,088,791-220,445,679 , GRCh38.p12 chr1: 219,915,449-220,272,337 AURKAP1, IARS2, 13 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 TGFB2, LOC105373475, 38 more genes
    nsv7095587copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,986,760 , GRCh38.p12 chr1: 219,915,449-220,813,418 BPNT1, SNORA36B, 24 more genes
    nsv7095586copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,101,782 , GRCh38.p12 chr1: 219,915,449-219,928,440 LOC107985281, SLC30A10
    nsv7095512copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,406,225 , GRCh38.p12 chr1: 219,915,449-220,232,883 MIR215, SNX2P1, 11 more genes
    nsv7055984inversion1nstd229human GRCh38 chr1: 219,905,257-219,912,637 , GRCh37.p13 chr1: 220,078,599-220,085,979 SLC30A10
    nsv7052462inversion1nstd229human GRCh38 chr1: 219,653,745-221,511,784 , GRCh37.p13 chr1: 219,827,087-221,685,126 RNA5SP76, MIR215, 36 more genes
    nsv6674680copy number variation1nstd229human GRCh38 chr1: 219,833,923-219,912,491 , GRCh37.p13 chr1: 220,007,265-220,085,833 SLC30A10, LOC105372926
    nsv6673024copy number variation1nstd229human GRCh38 chr1: 219,953,335-219,954,434 , GRCh37.p13 chr1: 220,126,677-220,127,776 SLC30A10
    nsv6670838copy number variation1nstd229human GRCh38 chr1: 219,950,464-219,953,316 , GRCh37.p13 chr1: 220,123,806-220,126,658 SLC30A10
    nsv6667869copy number variation1nstd229human GRCh38 chr1: 219,909,701-219,935,000 , GRCh37.p13 chr1: 220,083,043-220,108,342 LOC107985281, SLC30A10
    nsv6665947copy number variation1nstd229human GRCh38 chr1: 219,914,019-219,942,117 , GRCh37.p13 chr1: 220,087,361-220,115,459 SLC30A10, LOC107985281
    nsv6663483copy number variation1nstd229human GRCh38 chr1: 219,935,074-219,935,499 , GRCh37.p13 chr1: 220,108,416-220,108,841 SLC30A10, LOC107985281
    nsv6662696copy number variation1nstd229human GRCh38 chr1: 219,950,458-219,953,323 , GRCh37.p13 chr1: 220,123,800-220,126,665 SLC30A10
    nsv6661001copy number variation1nstd229human GRCh38 chr1: 219,950,409-219,953,367 , GRCh37.p13 chr1: 220,123,751-220,126,709 SLC30A10
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6626199copy number variation1nstd224human GRCh37 chr1: 220,089,014-220,119,384 , GRCh38.p12 chr1: 219,915,672-219,946,042 SLC30A10, LOC107985281
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